Login / Signup

Clinical Outcomes of an Innovative Cefazolin Delivery Program for MSSA Infections in OPAT.

Laura Herrera-HidalgoRafael Luque-MárquezAristides de AlarconAna Belén Guisado-GilBelen Gutierrez-GutierrezMaria Dolores Navarro-AmuedoJulia Praena-SegoviaJuan Manuel Carmona-CaballeroElena Fraile-RamosAlicia Gutierrez-ValenciaLuis Eduardo Lopez-CortesMaria Victoria Gil-Navarro
Published in: Journal of clinical medicine (2022)
Cefazolin is a recommended treatment for methicillin-susceptible Staphylococcus aureus (MSSA) infections that has been successfully used in outpatient parenteral antibiotic therapy (OPAT) programs. The aim of this study was to assess the clinical outcomes of cefazolin delivered each day (Group 24) vs. every two days (Group 48) for MSSA infections in OPAT programs. It was a prospective observational study with retrospective analysis of a cohort of MSSA infections attended in OPAT. The primary outcome was treatment success, defined as completing the antimicrobial regimen without death, treatment discontinuation, or readmission during treatment and follow-up. A univariate and multivariate logistic regression model was built. A two-sided p < 0.05 was considered statistically significant. Of the 149 MSSA infections treated with cefazolin 2 g/8 h in OPATs, 94 and 55 patients were included in the delivery Group 24 and Group 48, respectively. Treatment failure and unplanned readmission rates were similar in both groups (11.7% vs. 7.3% p = 0.752 and 8.5% vs. 5.5% p = 0.491). There was a significant increase in vascular access complications in Group 24 (33.0%) with respect to Group 48 (7.3%) ( p < 0.001). Treating uncomplicated MSSA infection with cefazolin home-delivered every two days through an OPAT program is not associated with an increased risk of treatment failure and entails a significant reduction in resource consumption compared to daily delivery.
Keyphrases
  • staphylococcus aureus
  • public health
  • healthcare
  • escherichia coli
  • combination therapy
  • cross sectional
  • pseudomonas aeruginosa
  • risk factors
  • cystic fibrosis
  • methicillin resistant staphylococcus aureus